The purpose of this pilot clinical trial is to evaluate the feasibility of the use of low-level laser for head and neck cancer survivors with lymphedema.
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Number of Participants Consented and Enrolled in Study
Timeframe: Approximately 5-month recruitment window
Number of Participants Completed the Study Visits
Timeframe: Approximately 10 weeks, from baseline visit to 4-week post-intervention visit
Number of Participants With Adverse Events
Timeframe: Approximately 10 weeks, from baseline visit to 4-week post-intervention visit
Number of Participants Who Were Satisfied With Study Intervention.
Timeframe: at 4-week post-intervention visit